Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285525 |
| ensemblid | ENSG00000177752.15 |
| hgncid | 26825 |
| symbol | YIPF7 |
| name | Yip1 domain family member 7 |
| refseq_nuc | NM_182592.3 |
| refseq_prot | NP_872398.3 |
| ensembl_nuc | ENST00000415895.9 |
| ensembl_prot | ENSP00000412696.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 44622088 |
| end | 44651625 |
| strand | - |
| ver | v1.2 |
| region | chr4:44622088-44651625 |
| region5000 | chr4:44617088-44656625 |
| regionname0 | YIPF7_chr4_44622088_44651625 |
| regionname5000 | YIPF7_chr4_44617088_44656625 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 256 | 330 | 87 | 57 | 131 | 15 | 38 | 103 | YIPF7_chr4_44617088_44656625 | YIPF7 | MSNLA others(251): Show |
chr4 | 44617088 | 44656625 |
| a0002 | 0/0 | 256 | 76 | 3 | 17 | 53 | 1 | 2 | 35 | YIPF7_chr4_44617088_44656625 | YIPF7 | MSNLA others(251): Show |
chr4 | 44617088 | 44656625 |
| a0003 | 0/0 | 256 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | MSNLA others(251): Show |
chr4 | 44617088 | 44656625 |
| a0004 | 0/0 | 67 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | MSNLA others(62): Show |
chr4 | 44617088 | 44656625 |
| a0005 | 0/0 | 256 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | MSNLA others(251): Show |
chr4 | 44617088 | 44656625 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 768 | 176 | 61 | 23 | 64 | 3 | 24 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0001c0002 | 1/0 | 768 | 146 | 26 | 34 | 59 | 12 | 14 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0001c0004 | 0/0 | 768 | 7 | 0 | 0 | 7 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0001c0006 | 0/0 | 768 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0002c0003 | 0/0 | 768 | 76 | 3 | 17 | 53 | 1 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0003c0005 | 0/0 | 768 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0004c0008 | 0/0 | 768 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 | ||
| a0005c0007 | 0/0 | 768 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | ATGTC others(763): Show |
chr4 | 44617088 | 44656625 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1169 | 162 | 47 | 23 | 64 | 3 | 24 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0001c0001t0004 | 0/0 | 1169 | 13 | 13 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0001c0001t0006 | 0/0 | 1169 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0001c0002t0002 | 1/0 | 1169 | 146 | 26 | 34 | 59 | 12 | 14 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0001c0004t0002 | 0/0 | 1169 | 7 | 0 | 0 | 7 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0001c0006t0002 | 0/0 | 1169 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0002c0003t0001 | 0/0 | 1169 | 39 | 3 | 6 | 29 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0002c0003t0003 | 0/0 | 1169 | 35 | 0 | 11 | 22 | 0 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0002c0003t0005 | 0/0 | 1169 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0003c0005t0002 | 0/0 | 1169 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0004c0008t0002 | 0/0 | 1169 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| a0005c0007t0001 | 0/0 | 1169 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | AATGG others(1164): Show |
chr4 | 44617088 | 44656625 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 3 | 7 | 1 | 4 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0005 | 0/0 | 11 | 6 | 2 | 0 | 1 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 0 | 6 | 1 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0001 | 0/0 | 22 | 1 | 6 | 11 | 2 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0007 | 0/0 | 9 | 0 | 2 | 5 | 1 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0011 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0016 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0029 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0004t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0001c0006t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0002 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0002c0003t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0003c0005t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0003c0005t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0004c0008t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| a0005c0007t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0104 | EUR | GBR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | FIN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0197 | EUR | FIN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0198 | EUR | FIN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0166 | EUR | FIN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00558 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01081 | hp2 | a0002 | c0003 | t0003 | g0027 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0010 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01358 | hp1 | a0002 | c0003 | t0003 | g0142 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01358 | hp2 | a0002 | c0003 | t0003 | g0010 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01496 | hp2 | a0002 | c0003 | t0003 | g0013 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0200 | EUR | IBS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0192 | EUR | IBS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0204 | EUR | IBS | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0043 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0150 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0013 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0149 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0144 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0145 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0139 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02004 | hp2 | a0002 | c0003 | t0003 | g0013 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0103 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02027 | hp1 | a0001 | c0006 | t0002 | g0172 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02083 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0043 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02165 | hp1 | a0002 | c0003 | t0003 | g0105 | EAS | CDX | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02273 | hp2 | a0002 | c0003 | t0003 | g0010 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02523 | hp2 | a0002 | c0003 | t0003 | g0013 | EAS | KHV | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0153 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02735 | hp2 | a0002 | c0003 | t0003 | g0107 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0191 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02922 | hp1 | a0004 | c0008 | t0002 | g0182 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0141 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0138 | AFR | ESN | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0164 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0106 | SAS | STU | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0151 | EAS | CHB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | CHB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | YRI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0108 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18963 | hp2 | a0002 | c0003 | t0003 | g0100 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18966 | hp2 | a0002 | c0003 | t0003 | g0101 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18974 | hp1 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18974 | hp2 | a0002 | c0003 | t0003 | g0099 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18975 | hp1 | a0002 | c0003 | t0003 | g0098 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18978 | hp2 | a0003 | c0005 | t0002 | g0189 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18980 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18981 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18993 | hp2 | a0002 | c0003 | t0005 | g0036 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18994 | hp2 | a0002 | c0003 | t0005 | g0036 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18995 | hp2 | a0001 | c0004 | t0002 | g0163 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18998 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0140 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19001 | hp1 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19005 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19010 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19012 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0185 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19059 | hp2 | a0001 | c0004 | t0002 | g0154 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19065 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19066 | hp2 | a0002 | c0003 | t0003 | g0097 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19075 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19075 | hp2 | a0003 | c0005 | t0002 | g0190 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19076 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19078 | hp2 | a0001 | c0004 | t0002 | g0217 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0102 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19082 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19089 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | YRI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ASW | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0169 | EUR | TSI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0196 | EUR | TSI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0044 | EUR | TSI | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | CLM | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0148 | AFR | USA | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| NA21309 | hp2 | a0005 | c0007 | t0001 | g0133 | AFR | LWK | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0059 | REF | REF | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0093 | REF | REF | YIPF7_chr4_44617088_44656625 | YIPF7 | chr4 | 44617088 | 44656625 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44624665 | C | T | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.544G>A | p.Val182Met | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/6 | 617/1170 | 544/771 | 182/256 | chr4 | 44624665 | |||
| chr4:44629426 | C | A | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.403G>T | p.Ala135Ser | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/6 | 476/1170 | 403/771 | 135/256 | chr4 | 44629426 | |||
| chr4:44635937 | G | T | 1 | a0003 | 2 | NA18978.hp2 NA19075.hp2 |
missense_variant | MODERATE | c.265C>A | p.Pro89Thr | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/6 | 338/1170 | 265/771 | 89/256 | chr4 | 44635937 | |||
| chr4:44636000 | G | A | 1 | a0004 | 1 | HG02922.hp1 | stop_gained | HIGH | c.202C>T | p.Gln68* | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/6 | 275/1170 | 202/771 | 68/256 | chr4 | 44636000 | |||
| chr4:44650013 | C | T | 1 | a0002 | 76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
missense_variant | MODERATE | c.88G>A | p.Ala30Thr | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/6 | 161/1170 | 88/771 | 30/256 | chr4 | 44650013 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44624621 | G | A | 1 | a0001c0004 | 7 | NA18974.hp1 NA18995.hp2 NA19001.hp1 others(4): Show |
synonymous_variant | LOW | c.588C>T | p.Cys196Cys | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/6 | 661/1170 | 588/771 | 196/256 | chr4 | 44624621 | |||
| chr4:44624624 | A | G | 3 | a0001c0001 a0002c0003 a0005c0007 |
252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
synonymous_variant | LOW | c.585T>C | p.Gly195Gly | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/6 | 658/1170 | 585/771 | 195/256 | chr4 | 44624624 | |||
| chr4:44629448 | A | G | 1 | a0001c0006 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.381T>C | p.Thr127Thr | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/6 | 454/1170 | 381/771 | 127/256 | chr4 | 44629448 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44622139 | C | A | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(4): Show |
252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*275G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 275 | chr4 | 44622139 | ||||||
| chr4:44622160 | T | C | 2 | a0002c0003t0003 a0002c0003t0005 |
37 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*254A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 254 | chr4 | 44622160 | ||||||
| chr4:44622179 | A | T | 1 | a0001c0001t0004 | 13 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*235T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 235 | chr4 | 44622179 | ||||||
| chr4:44622183 | C | T | 1 | a0001c0001t0004 | 13 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 231 | chr4 | 44622183 | ||||||
| chr4:44622335 | C | T | 1 | a0002c0003t0005 | 2 | NA18993.hp2 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*79G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 79 | chr4 | 44622335 | ||||||
| chr4:44622373 | G | T | 1 | a0001c0001t0006 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 6/6 | 41 | chr4 | 44622373 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44622601 | T | G | 2 | a0001c0001t0004g0232 a0001c0001t0004g0234 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.609-25A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44622601 | |||||||
| chr4:44622683 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0127 others(1): Show |
4 | NA18948.hp1 NA18962.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-107C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44622683 | |||||||
| chr4:44622764 | G | C | 1 | a0005c0007t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.609-188C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44622764 | |||||||
| chr4:44622791 | C | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(42): Show |
79 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.609-215G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44622791 | |||||||
| chr4:44622959 | G | A | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609-383C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44622959 | |||||||
| chr4:44623005 | C | A | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.609-429G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623005 | |||||||
| chr4:44623403 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.609-827G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623403 | |||||||
| chr4:44623470 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.609-894A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623470 | |||||||
| chr4:44623683 | T | A | 1 | a0001c0002t0002g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.608+918A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623683 | |||||||
| chr4:44623704 | G | A | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.608+897C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623704 | |||||||
| chr4:44623850 | G | A | 5 | a0002c0003t0001g0043 a0002c0003t0001g0144 a0002c0003t0001g0145 others(2): Show |
6 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.608+751C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623850 | |||||||
| chr4:44623858 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0064 a0001c0001t0001g0089 others(1): Show |
5 | HG02572.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+743C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44623858 | |||||||
| chr4:44624050 | TTCTC | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.608+547_608+550del others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624050 | |||||||
| chr4:44624060 | C | CT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0111 others(3): Show |
7 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+540dupA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624060 | |||||||
| chr4:44624060 | CT | C | 7 | a0001c0001t0001g0110 a0001c0001t0001g0131 a0001c0001t0004g0235 others(4): Show |
7 | HG01167.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+540delA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624060 | |||||||
| chr4:44624086 | G | A | 33 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0031 others(30): Show |
41 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.608+515C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624086 | |||||||
| chr4:44624132 | C | T | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.608+469G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624132 | |||||||
| chr4:44624167 | C | T | 1 | a0002c0003t0001g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.608+434G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624167 | |||||||
| chr4:44624216 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
6 | HG01167.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.608+385G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624216 | |||||||
| chr4:44624222 | G | A | 1 | a0001c0002t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.608+379C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624222 | |||||||
| chr4:44624275 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.608+326C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624275 | |||||||
| chr4:44624291 | C | T | 1 | a0002c0003t0001g0138 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.608+310G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624291 | |||||||
| chr4:44624339 | C | T | 21 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(18): Show |
42 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.608+262G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624339 | |||||||
| chr4:44624356 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0064 |
3 | HG02622.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.608+245C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624356 | |||||||
| chr4:44624359 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.608+242A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624359 | |||||||
| chr4:44624479 | T | C | 1 | a0002c0003t0001g0138 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.608+122A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624479 | |||||||
| chr4:44624569 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0064 a0001c0001t0001g0089 others(1): Show |
5 | HG02572.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+32A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624569 | |||||||
| chr4:44624582 | A | G | 1 | a0002c0003t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.608+19T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 5/5 | chr4 | 44624582 | |||||||
| chr4:44624789 | C | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
splice_region_variant&intron_variant | LOW | c.427-7G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44624789 | |||||||
| chr4:44624820 | A | G | 1 | a0002c0003t0001g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.427-38T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44624820 | |||||||
| chr4:44624829 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
252 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.427-47C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44624829 | |||||||
| chr4:44625127 | A | T | 4 | a0001c0004t0002g0015 a0001c0004t0002g0154 a0001c0004t0002g0163 others(1): Show |
7 | NA18974.hp1 NA18995.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.427-345T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625127 | |||||||
| chr4:44625249 | G | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.427-467C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625249 | |||||||
| chr4:44625293 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.427-511G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625293 | |||||||
| chr4:44625336 | C | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.427-554G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625336 | |||||||
| chr4:44625511 | A | G | 2 | a0001c0002t0002g0168 a0001c0002t0002g0171 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.427-729T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625511 | |||||||
| chr4:44625521 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0067 |
4 | HG01981.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-739T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625521 | |||||||
| chr4:44625800 | G | A | 3 | a0001c0002t0002g0226 a0001c0002t0002g0227 a0001c0002t0002g0228 |
3 | HG02027.hp2 NA18980.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.427-1018C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625800 | |||||||
| chr4:44625863 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-1081G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625863 | |||||||
| chr4:44625867 | T | G | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-1085A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625867 | |||||||
| chr4:44625980 | C | T | 4 | a0001c0002t0002g0046 a0001c0002t0002g0185 a0001c0002t0002g0187 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-1198G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44625980 | |||||||
| chr4:44626222 | GT | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.427-1441delA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626222 | |||||||
| chr4:44626254 | A | G | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.427-1472T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626254 | |||||||
| chr4:44626313 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427-1531G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626313 | |||||||
| chr4:44626388 | G | T | 1 | a0001c0002t0002g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.427-1606C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626388 | |||||||
| chr4:44626550 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.427-1768A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626550 | |||||||
| chr4:44626574 | C | G | 1 | a0002c0003t0001g0147 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.427-1792G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626574 | |||||||
| chr4:44626590 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.427-1808G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626590 | |||||||
| chr4:44626681 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0006g0112 |
3 | HG02723.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.427-1899T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626681 | |||||||
| chr4:44626719 | CA | C | 17 | a0002c0003t0003g0009 a0002c0003t0003g0010 a0002c0003t0003g0013 others(14): Show |
33 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.427-1938delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626719 | |||||||
| chr4:44626763 | C | CT | 5 | a0001c0001t0001g0064 a0001c0001t0001g0214 a0001c0001t0004g0052 others(2): Show |
6 | HG02559.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1982dupA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0058 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.427-1983_427-1982d others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTTT | 13 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0002t0002g0016 others(10): Show |
18 | HG00733.hp2 HG01256.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.427-1984_427-1982d others(5): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTTTT | 41 | a0001c0002t0002g0001 a0001c0002t0002g0011 a0001c0002t0002g0026 others(38): Show |
76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.427-1985_427-1982d others(6): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTTTTT | 28 | a0001c0002t0002g0007 a0001c0002t0002g0017 a0001c0002t0002g0025 others(25): Show |
43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.427-1986_427-1982d others(7): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTTTTTT | 7 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0191 others(4): Show |
11 | HG01175.hp1 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-1987_427-1982d others(8): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | CTTTTTTT | 4 | a0001c0001t0001g0055 a0001c0002t0002g0029 a0001c0002t0002g0173 others(1): Show |
6 | HG01975.hp2 HG02148.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1988_427-1982d others(9): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | C | T | 1 | a0001c0002t0002g0096 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.427-1981G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | CTTTTT | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0082 a0001c0001t0001g0109 others(3): Show |
7 | HG01255.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-1986_427-1982d others(7): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | CTTTTTTT | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(29): Show |
50 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.427-1988_427-1982d others(9): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | CTTTTTTT others(1): Show |
C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.427-1989_427-1982d others(10): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0067 a0001c0001t0001g0076 others(2): Show |
6 | HG00639.hp2 HG01168.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1990_427-1982d others(11): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626763 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.427-1991_427-1982d others(12): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626763 | |||||||
| chr4:44626795 | T | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
227 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.427-2013A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626795 | |||||||
| chr4:44626823 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0087 |
5 | HG01993.hp2 HG02647.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.427-2041G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626823 | |||||||
| chr4:44626864 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.427-2082G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626864 | |||||||
| chr4:44626896 | C | A | 1 | a0002c0003t0003g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.427-2114G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626896 | |||||||
| chr4:44626903 | G | A | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.427-2121C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626903 | |||||||
| chr4:44626911 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0135 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.427-2129C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626911 | |||||||
| chr4:44626922 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.427-2140G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626922 | |||||||
| chr4:44626951 | A | AT | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0023 others(87): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.427-2170dupA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626951 | |||||||
| chr4:44626951 | A | ATT | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(34): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.427-2171_427-2170d others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626951 | |||||||
| chr4:44626951 | A | C | 1 | a0001c0002t0002g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.427-2169T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44626951 | |||||||
| chr4:44627009 | C | T | 2 | a0001c0002t0002g0183 a0001c0002t0002g0184 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.427-2227G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627009 | |||||||
| chr4:44627029 | G | A | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.427-2247C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627029 | |||||||
| chr4:44627067 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.427-2285G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627067 | |||||||
| chr4:44627081 | C | T | 1 | a0001c0002t0002g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427-2299G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627081 | |||||||
| chr4:44627186 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.426+2217G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627186 | |||||||
| chr4:44627309 | C | T | 3 | a0001c0002t0002g0176 a0001c0002t0002g0207 a0001c0002t0002g0208 |
3 | HG00438.hp1 NA18972.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.426+2094G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627309 | |||||||
| chr4:44627358 | T | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
40 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.426+2045A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627358 | |||||||
| chr4:44627400 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.426+2003A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627400 | |||||||
| chr4:44627408 | G | T | 1 | a0002c0003t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.426+1995C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627408 | |||||||
| chr4:44627568 | T | C | 17 | a0002c0003t0003g0009 a0002c0003t0003g0010 a0002c0003t0003g0013 others(14): Show |
33 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.426+1835A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627568 | |||||||
| chr4:44627625 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.426+1778C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627625 | |||||||
| chr4:44627725 | A | C | 21 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(18): Show |
42 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.426+1678T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627725 | |||||||
| chr4:44627863 | A | C | 20 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(17): Show |
41 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.426+1540T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44627863 | |||||||
| chr4:44628384 | TA | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.426+1018delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628384 | |||||||
| chr4:44628409 | T | A | 17 | a0002c0003t0003g0009 a0002c0003t0003g0010 a0002c0003t0003g0013 others(14): Show |
33 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.426+994A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628409 | |||||||
| chr4:44628531 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.426+872A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628531 | |||||||
| chr4:44628542 | G | A | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.426+861C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628542 | |||||||
| chr4:44628633 | GTCAGAGA others(7): Show |
G | 64 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.426+756_426+769del others(14): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628633 | |||||||
| chr4:44628769 | T | A | 1 | a0001c0002t0002g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.426+634A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628769 | |||||||
| chr4:44628816 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.426+587T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628816 | |||||||
| chr4:44628927 | T | C | 92 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0011 others(89): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.426+476A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628927 | |||||||
| chr4:44628960 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.426+443G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44628960 | |||||||
| chr4:44629151 | C | CT | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.426+251_426+252ins others(1): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44629151 | |||||||
| chr4:44629244 | T | C | 9 | a0002c0003t0003g0009 a0002c0003t0003g0010 a0002c0003t0003g0098 others(6): Show |
20 | HG00544.hp1 HG00673.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+159A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 4/5 | chr4 | 44629244 | |||||||
| chr4:44629570 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-22T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629570 | |||||||
| chr4:44629581 | A | G | 1 | a0001c0002t0002g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.281-33T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629581 | |||||||
| chr4:44629711 | A | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
40 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.281-163T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629711 | |||||||
| chr4:44629728 | CAT | C | 91 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0011 others(88): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.281-182_281-181del others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629728 | |||||||
| chr4:44629768 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.281-220G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629768 | |||||||
| chr4:44629883 | G | A | 1 | a0001c0002t0002g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.281-335C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629883 | |||||||
| chr4:44629939 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-391C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629939 | |||||||
| chr4:44629998 | G | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.281-450C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44629998 | |||||||
| chr4:44630043 | C | T | 1 | a0002c0003t0003g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.281-495G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630043 | |||||||
| chr4:44630382 | T | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.281-834A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630382 | |||||||
| chr4:44630560 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.281-1012C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630560 | |||||||
| chr4:44630781 | A | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
6 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-1233T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630781 | |||||||
| chr4:44630825 | G | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
40 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.281-1277C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630825 | |||||||
| chr4:44630888 | T | C | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.281-1340A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44630888 | |||||||
| chr4:44631126 | T | C | 1 | a0001c0002t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.281-1578A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631126 | |||||||
| chr4:44631177 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0073 |
4 | HG00438.hp2 NA18939.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-1629G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631177 | |||||||
| chr4:44631178 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281-1630A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631178 | |||||||
| chr4:44631207 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.281-1659C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631207 | |||||||
| chr4:44631241 | T | A | 1 | a0001c0002t0002g0195 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-1693A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631241 | |||||||
| chr4:44631367 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-1819C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631367 | |||||||
| chr4:44631383 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0064 |
3 | HG02622.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.281-1835A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631383 | |||||||
| chr4:44631399 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.281-1851C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631399 | |||||||
| chr4:44631436 | A | C | 1 | a0002c0003t0003g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.281-1888T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631436 | |||||||
| chr4:44631662 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0130 |
2 | NA19005.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.281-2114A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631662 | |||||||
| chr4:44631678 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.281-2130T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631678 | |||||||
| chr4:44631682 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0131 |
4 | HG02135.hp1 HG02155.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-2134T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631682 | |||||||
| chr4:44631719 | G | A | 7 | a0001c0002t0002g0028 a0001c0002t0002g0155 a0001c0002t0002g0156 others(4): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-2171C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631719 | |||||||
| chr4:44631764 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2216C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631764 | |||||||
| chr4:44631788 | T | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2240A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631788 | |||||||
| chr4:44631834 | A | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0127 others(1): Show |
4 | NA18948.hp1 NA18962.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-2286T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631834 | |||||||
| chr4:44631837 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2289T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631837 | |||||||
| chr4:44631849 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.281-2301C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631849 | |||||||
| chr4:44631878 | G | A | 1 | a0001c0002t0002g0178 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.281-2330C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631878 | |||||||
| chr4:44631892 | T | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.281-2344A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631892 | |||||||
| chr4:44631995 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2447C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44631995 | |||||||
| chr4:44632045 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2497A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632045 | |||||||
| chr4:44632057 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2509C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632057 | |||||||
| chr4:44632118 | TTGTA | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2574_281-2571d others(6): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632118 | |||||||
| chr4:44632142 | G | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2594C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632142 | |||||||
| chr4:44632181 | T | C | 1 | a0001c0002t0002g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.281-2633A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632181 | |||||||
| chr4:44632203 | T | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2655A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632203 | |||||||
| chr4:44632240 | T | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2692A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632240 | |||||||
| chr4:44632349 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2801G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632349 | |||||||
| chr4:44632388 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2840C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632388 | |||||||
| chr4:44632397 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-2849C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632397 | |||||||
| chr4:44632441 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(115): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.281-2893C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632441 | |||||||
| chr4:44632606 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.281-3058T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632606 | |||||||
| chr4:44632616 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-3068T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632616 | |||||||
| chr4:44632619 | G | A | 1 | a0001c0002t0002g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.281-3071C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632619 | |||||||
| chr4:44632664 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-3116T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632664 | |||||||
| chr4:44632666 | A | T | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.281-3118T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632666 | |||||||
| chr4:44632843 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+3079C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632843 | |||||||
| chr4:44632896 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+3026C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632896 | |||||||
| chr4:44632906 | C | G | 38 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(35): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.280+3016G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632906 | |||||||
| chr4:44632944 | C | T | 1 | a0002c0003t0001g0042 | 2 | HG00408.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.280+2978G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632944 | |||||||
| chr4:44632966 | AGCAGTGG | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
7 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+2949_280+2955d others(9): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44632966 | |||||||
| chr4:44633059 | T | C | 1 | a0001c0002t0002g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+2863A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633059 | |||||||
| chr4:44633090 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280+2832G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633090 | |||||||
| chr4:44633140 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.280+2782C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633140 | |||||||
| chr4:44633260 | T | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
47 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+2662A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633260 | |||||||
| chr4:44633271 | C | A | 1 | a0001c0002t0002g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.280+2651G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633271 | |||||||
| chr4:44633400 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
47 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+2522G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633400 | |||||||
| chr4:44633431 | T | A | 3 | a0002c0003t0003g0099 a0002c0003t0003g0100 a0002c0003t0003g0101 |
3 | NA18963.hp2 NA18966.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.280+2491A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633431 | |||||||
| chr4:44633448 | AAT | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
47 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+2472_280+2473d others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633448 | |||||||
| chr4:44633450 | TA | T | 17 | a0002c0003t0003g0009 a0002c0003t0003g0010 a0002c0003t0003g0013 others(14): Show |
33 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+2471delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633450 | |||||||
| chr4:44633471 | T | C | 1 | a0001c0002t0002g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.280+2451A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633471 | |||||||
| chr4:44633518 | A | T | 1 | a0001c0001t0001g0034 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.280+2404T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633518 | |||||||
| chr4:44633543 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.280+2379A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633543 | |||||||
| chr4:44633575 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
47 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+2347A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633575 | |||||||
| chr4:44633640 | G | A | 1 | a0001c0002t0002g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+2282C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633640 | |||||||
| chr4:44633645 | G | A | 2 | a0002c0003t0003g0103 a0002c0003t0003g0105 |
2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.280+2277C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633645 | |||||||
| chr4:44633720 | G | GA | 93 | a0001c0001t0004g0236 a0001c0002t0002g0001 a0001c0002t0002g0007 others(90): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.280+2201dupT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633720 | |||||||
| chr4:44633784 | A | G | 94 | a0001c0001t0004g0209 a0001c0001t0004g0210 a0001c0002t0002g0001 others(91): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.280+2138T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633784 | |||||||
| chr4:44633807 | C | T | 2 | a0002c0003t0003g0027 a0002c0003t0003g0142 |
4 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+2115G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633807 | |||||||
| chr4:44633832 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
6 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+2090T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44633832 | |||||||
| chr4:44634109 | T | C | 2 | a0002c0003t0001g0144 a0002c0003t0001g0150 |
2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.280+1813A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634109 | |||||||
| chr4:44634138 | C | T | 21 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(18): Show |
42 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.280+1784G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634138 | |||||||
| chr4:44634176 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
47 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+1746C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634176 | |||||||
| chr4:44634432 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+1490G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634432 | |||||||
| chr4:44634446 | C | T | 1 | a0001c0002t0002g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.280+1476G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634446 | |||||||
| chr4:44634470 | T | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280+1452A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634470 | |||||||
| chr4:44634505 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
40 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.280+1417G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634505 | |||||||
| chr4:44634604 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0077 others(1): Show |
14 | HG02080.hp2 NA18946.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.280+1318A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634604 | |||||||
| chr4:44634992 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.280+930T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44634992 | |||||||
| chr4:44635147 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG02071.hp2 HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.280+775C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635147 | |||||||
| chr4:44635222 | A | G | 2 | a0002c0003t0001g0137 a0002c0003t0001g0152 |
2 | NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.280+700T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635222 | |||||||
| chr4:44635319 | G | A | 3 | a0001c0002t0002g0047 a0001c0002t0002g0153 a0001c0002t0002g0175 |
4 | HG00733.hp2 HG01256.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+603C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635319 | |||||||
| chr4:44635398 | C | T | 1 | a0002c0003t0001g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.280+524G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635398 | |||||||
| chr4:44635461 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.280+461T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635461 | |||||||
| chr4:44635719 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.280+203A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635719 | |||||||
| chr4:44635805 | T | C | 2 | a0001c0002t0002g0197 a0001c0002t0002g0198 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.280+117A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635805 | |||||||
| chr4:44635834 | C | T | 38 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(35): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.280+88G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 3/5 | chr4 | 44635834 | |||||||
| chr4:44636143 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.117-58C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636143 | |||||||
| chr4:44636288 | G | A | 67 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0011 others(64): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.117-203C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636288 | |||||||
| chr4:44636502 | G | A | 89 | a0001c0001t0001g0188 a0001c0002t0002g0001 a0001c0002t0002g0007 others(86): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.117-417C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636502 | |||||||
| chr4:44636536 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0131 |
4 | HG02135.hp1 HG02155.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-451C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636536 | |||||||
| chr4:44636601 | T | C | 39 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(36): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.117-516A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636601 | |||||||
| chr4:44636603 | G | A | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.117-518C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636603 | |||||||
| chr4:44636608 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0067 |
4 | HG01981.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-523C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636608 | |||||||
| chr4:44636681 | C | T | 1 | a0004c0008t0002g0182 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.117-596G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636681 | |||||||
| chr4:44636723 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0068 |
7 | HG00673.hp2 HG02129.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.117-638G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636723 | |||||||
| chr4:44636914 | C | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.117-829G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636914 | |||||||
| chr4:44636965 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
48 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.117-880C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636965 | |||||||
| chr4:44636977 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.117-892G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44636977 | |||||||
| chr4:44637258 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0074 |
3 | HG03710.hp2 HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.117-1173A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637258 | |||||||
| chr4:44637261 | C | G | 3 | a0001c0002t0002g0180 a0001c0002t0002g0181 a0001c0002t0002g0206 |
3 | NA18946.hp1 NA18985.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.117-1176G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637261 | |||||||
| chr4:44637294 | C | T | 91 | a0001c0001t0001g0188 a0001c0001t0004g0209 a0001c0001t0004g0210 others(88): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.117-1209G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637294 | |||||||
| chr4:44637319 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.117-1234A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637319 | |||||||
| chr4:44637430 | G | A | 1 | a0005c0007t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117-1345C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637430 | |||||||
| chr4:44637453 | T | A | 91 | a0001c0001t0001g0188 a0001c0001t0004g0209 a0001c0001t0004g0210 others(88): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.117-1368A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637453 | |||||||
| chr4:44637500 | T | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.117-1415A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637500 | |||||||
| chr4:44637520 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.117-1435T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637520 | |||||||
| chr4:44637535 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.117-1450C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637535 | |||||||
| chr4:44637717 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.117-1632T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637717 | |||||||
| chr4:44637760 | C | T | 20 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(17): Show |
41 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.117-1675G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637760 | |||||||
| chr4:44637966 | T | C | 1 | a0001c0001t0001g0021 | 3 | NA18939.hp2 NA18948.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.117-1881A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637966 | |||||||
| chr4:44637982 | A | T | 1 | a0001c0002t0002g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.117-1897T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44637982 | |||||||
| chr4:44638027 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117-1942C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638027 | |||||||
| chr4:44638081 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.117-1996C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638081 | |||||||
| chr4:44638089 | A | C | 1 | a0001c0001t0004g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117-2004T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638089 | |||||||
| chr4:44638112 | G | A | 39 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(36): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.117-2027C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638112 | |||||||
| chr4:44638157 | GC | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(30): Show |
55 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.117-2073delG | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638157 | |||||||
| chr4:44638209 | AT | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
54 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.117-2125delA | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638209 | |||||||
| chr4:44638209 | ATT | A | 99 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0054 others(96): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.117-2126_117-2125d others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638209 | |||||||
| chr4:44638209 | ATTT | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
123 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.117-2127_117-2125d others(5): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638209 | |||||||
| chr4:44638209 | ATTTT | A | 33 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0075 others(30): Show |
56 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.117-2128_117-2125d others(6): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638209 | |||||||
| chr4:44638418 | C | T | 1 | a0002c0003t0003g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.117-2333G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638418 | |||||||
| chr4:44638425 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117-2340T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638425 | |||||||
| chr4:44638555 | T | A | 89 | a0001c0001t0001g0188 a0001c0002t0002g0001 a0001c0002t0002g0007 others(86): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.117-2470A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44638555 | |||||||
| chr4:44639013 | T | C | 1 | a0002c0003t0001g0140 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.117-2928A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639013 | |||||||
| chr4:44639129 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.117-3044G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639129 | |||||||
| chr4:44639190 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.117-3105A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639190 | |||||||
| chr4:44639193 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117-3108C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639193 | |||||||
| chr4:44639267 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.117-3182T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639267 | |||||||
| chr4:44639375 | T | G | 194 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(191): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.117-3290A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639375 | |||||||
| chr4:44639777 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.117-3692T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639777 | |||||||
| chr4:44639778 | GA | G | 94 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(91): Show |
158 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.117-3694delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44639778 | |||||||
| chr4:44640101 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.117-4016C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640101 | |||||||
| chr4:44640107 | G | A | 1 | a0001c0002t0002g0201 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.117-4022C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640107 | |||||||
| chr4:44640221 | C | T | 1 | a0001c0006t0002g0172 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.117-4136G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640221 | |||||||
| chr4:44640296 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.117-4211T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640296 | |||||||
| chr4:44640418 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.117-4333T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640418 | |||||||
| chr4:44640436 | C | T | 100 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(97): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.117-4351G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640436 | |||||||
| chr4:44640698 | C | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-4613G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640698 | |||||||
| chr4:44640705 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.117-4620G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640705 | |||||||
| chr4:44640780 | C | A | 1 | a0001c0002t0002g0048 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.117-4695G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640780 | |||||||
| chr4:44640947 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-4862C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640947 | |||||||
| chr4:44640978 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
48 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.117-4893G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44640978 | |||||||
| chr4:44641079 | G | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(30): Show |
55 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.117-4994C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641079 | |||||||
| chr4:44641202 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
48 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.117-5117G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641202 | |||||||
| chr4:44641365 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.117-5280G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641365 | |||||||
| chr4:44641524 | C | T | 39 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(36): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.117-5439G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641524 | |||||||
| chr4:44641627 | G | A | 1 | a0001c0002t0002g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.117-5542C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641627 | |||||||
| chr4:44641668 | A | T | 1 | a0005c0007t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117-5583T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641668 | |||||||
| chr4:44641758 | C | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.117-5673G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641758 | |||||||
| chr4:44641806 | A | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(30): Show |
55 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.117-5721T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641806 | |||||||
| chr4:44641937 | C | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.117-5852G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641937 | |||||||
| chr4:44641967 | T | C | 1 | a0001c0002t0002g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.117-5882A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641967 | |||||||
| chr4:44641995 | A | T | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.117-5910T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44641995 | |||||||
| chr4:44642411 | T | G | 88 | a0001c0001t0001g0188 a0001c0002t0002g0001 a0001c0002t0002g0007 others(85): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.117-6326A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642411 | |||||||
| chr4:44642446 | AC | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.117-6362delG | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642446 | |||||||
| chr4:44642470 | T | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.117-6385A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642470 | |||||||
| chr4:44642552 | A | G | 4 | a0001c0002t0002g0168 a0001c0002t0002g0169 a0001c0002t0002g0170 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.117-6467T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642552 | |||||||
| chr4:44642670 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.117-6585T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642670 | |||||||
| chr4:44642758 | G | A | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.117-6673C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642758 | |||||||
| chr4:44642773 | C | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.117-6688G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642773 | |||||||
| chr4:44642861 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117-6776C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642861 | |||||||
| chr4:44642943 | T | C | 8 | a0002c0003t0003g0013 a0002c0003t0003g0022 a0002c0003t0003g0097 others(5): Show |
13 | HG00558.hp2 HG01496.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.117-6858A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44642943 | |||||||
| chr4:44643011 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0077 others(1): Show |
14 | HG02080.hp2 NA18946.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.117-6926C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643011 | |||||||
| chr4:44643129 | A | C | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+6856T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643129 | |||||||
| chr4:44643140 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.116+6845A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643140 | |||||||
| chr4:44643203 | G | C | 6 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 others(3): Show |
9 | HG01109.hp1 HG01516.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+6782C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643203 | |||||||
| chr4:44643358 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116+6627G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643358 | |||||||
| chr4:44643394 | A | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.116+6591T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643394 | |||||||
| chr4:44643559 | A | G | 1 | a0001c0001t0001g0019 | 3 | NA18953.hp2 NA18978.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.116+6426T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643559 | |||||||
| chr4:44643563 | G | C | 1 | a0005c0007t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.116+6422C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643563 | |||||||
| chr4:44643662 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0080 |
3 | HG03654.hp2 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.116+6323G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643662 | |||||||
| chr4:44643766 | A | G | 4 | a0002c0003t0003g0022 a0002c0003t0003g0097 a0002c0003t0003g0102 others(1): Show |
6 | HG00558.hp2 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+6219T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643766 | |||||||
| chr4:44643780 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
6 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+6205T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643780 | |||||||
| chr4:44643789 | G | A | 1 | a0001c0002t0002g0205 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.116+6196C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643789 | |||||||
| chr4:44643857 | C | T | 1 | a0002c0003t0001g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.116+6128G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643857 | |||||||
| chr4:44643946 | G | A | 1 | a0005c0007t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.116+6039C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643946 | |||||||
| chr4:44643949 | G | A | 1 | a0001c0002t0002g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.116+6036C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643949 | |||||||
| chr4:44643989 | T | A | 100 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(97): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.116+5996A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44643989 | |||||||
| chr4:44644055 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0122 |
3 | HG01884.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116+5930C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644055 | |||||||
| chr4:44644080 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.116+5905G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644080 | |||||||
| chr4:44644126 | C | T | 91 | a0001c0001t0001g0188 a0001c0001t0004g0209 a0001c0001t0004g0210 others(88): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.116+5859G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644126 | |||||||
| chr4:44644142 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.116+5843C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644142 | |||||||
| chr4:44644303 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
6 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+5682T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644303 | |||||||
| chr4:44644317 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.116+5668G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644317 | |||||||
| chr4:44644414 | A | C | 1 | a0001c0002t0002g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.116+5571T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644414 | |||||||
| chr4:44644415 | C | A | 1 | a0001c0002t0002g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.116+5570G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644415 | |||||||
| chr4:44644480 | A | C | 1 | a0002c0003t0001g0140 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.116+5505T>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644480 | |||||||
| chr4:44644567 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0068 |
7 | HG00673.hp2 HG02129.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.116+5418C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644567 | |||||||
| chr4:44644686 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116+5299C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644686 | |||||||
| chr4:44644694 | G | A | 100 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(97): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.116+5291C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644694 | |||||||
| chr4:44644883 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0085 |
3 | HG01243.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.116+5102A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644883 | |||||||
| chr4:44644917 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.116+5068T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644917 | |||||||
| chr4:44644927 | G | C | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.116+5058C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44644927 | |||||||
| chr4:44645075 | G | A | 99 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(96): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.116+4910C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645075 | |||||||
| chr4:44645077 | G | T | 1 | a0001c0002t0002g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.116+4908C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645077 | |||||||
| chr4:44645085 | G | T | 39 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(36): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.116+4900C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645085 | |||||||
| chr4:44645115 | C | T | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+4870G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645115 | |||||||
| chr4:44645147 | G | A | 1 | a0001c0002t0002g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.116+4838C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645147 | |||||||
| chr4:44645288 | T | C | 1 | a0002c0003t0001g0138 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.116+4697A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645288 | |||||||
| chr4:44645397 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.116+4588C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645397 | |||||||
| chr4:44645401 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.116+4584G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645401 | |||||||
| chr4:44645491 | A | T | 4 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(1): Show |
4 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.116+4494T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645491 | |||||||
| chr4:44645744 | G | A | 18 | a0002c0003t0001g0104 a0002c0003t0003g0009 a0002c0003t0003g0010 others(15): Show |
34 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.116+4241C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44645744 | |||||||
| chr4:44646064 | C | A | 2 | a0001c0002t0002g0207 a0001c0002t0002g0208 |
2 | NA18972.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.116+3921G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646064 | |||||||
| chr4:44646119 | T | C | 1 | a0001c0002t0002g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.116+3866A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646119 | |||||||
| chr4:44646166 | T | C | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.116+3819A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646166 | |||||||
| chr4:44646217 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
48 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.116+3768T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646217 | |||||||
| chr4:44646312 | A | G | 1 | a0001c0004t0002g0163 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.116+3673T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646312 | |||||||
| chr4:44646316 | T | C | 2 | a0001c0002t0002g0211 a0001c0002t0002g0212 |
2 | NA18957.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.116+3669A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646316 | |||||||
| chr4:44646443 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0122 |
3 | HG01884.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116+3542C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646443 | |||||||
| chr4:44646615 | G | A | 1 | a0002c0003t0003g0108 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.116+3370C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646615 | |||||||
| chr4:44646658 | C | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
6 | HG00642.hp1 HG01123.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.116+3327G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646658 | |||||||
| chr4:44646780 | G | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(130): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.116+3205C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646780 | |||||||
| chr4:44646837 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.116+3148T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44646837 | |||||||
| chr4:44647093 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.116+2892C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647093 | |||||||
| chr4:44647107 | G | A | 1 | a0001c0001t0001g0024 | 3 | NA18968.hp2 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.116+2878C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647107 | |||||||
| chr4:44647158 | A | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.116+2827T>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647158 | |||||||
| chr4:44647342 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.116+2643G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647342 | |||||||
| chr4:44647489 | C | CTTAGTAG others(10): Show |
1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+2479_116+2495d others(19): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647489 | |||||||
| chr4:44647559 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.116+2426A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647559 | |||||||
| chr4:44647602 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+2383G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647602 | |||||||
| chr4:44647793 | C | T | 104 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0109 others(101): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.116+2192G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647793 | |||||||
| chr4:44647896 | A | ATG | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
49 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.116+2087_116+2088d others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647896 | |||||||
| chr4:44647983 | T | C | 1 | a0001c0002t0002g0216 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.116+2002A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44647983 | |||||||
| chr4:44648173 | T | C | 1 | a0002c0003t0001g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.116+1812A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648173 | |||||||
| chr4:44648212 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+1773A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648212 | |||||||
| chr4:44648213 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+1772C>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648213 | |||||||
| chr4:44648214 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+1771A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648214 | |||||||
| chr4:44648237 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0135 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.116+1748A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648237 | |||||||
| chr4:44648488 | A | G | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+1497T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648488 | |||||||
| chr4:44648506 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
5 | HG01981.hp2 HG03704.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.116+1479G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648506 | |||||||
| chr4:44648544 | C | T | 133 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(130): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.116+1441G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648544 | |||||||
| chr4:44648602 | T | G | 1 | a0001c0004t0002g0217 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.116+1383A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648602 | |||||||
| chr4:44648742 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.116+1243T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648742 | |||||||
| chr4:44648833 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.116+1152G>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648833 | |||||||
| chr4:44648959 | T | C | 20 | a0002c0003t0001g0002 a0002c0003t0001g0041 a0002c0003t0001g0042 others(17): Show |
41 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.116+1026A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648959 | |||||||
| chr4:44648990 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
49 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.116+995C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44648990 | |||||||
| chr4:44649043 | A | G | 1 | a0001c0002t0002g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.116+942T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649043 | |||||||
| chr4:44649123 | T | A | 1 | a0001c0001t0001g0024 | 3 | NA18968.hp2 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.116+862A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649123 | |||||||
| chr4:44649183 | G | C | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+802C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649183 | |||||||
| chr4:44649248 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.116+737C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649248 | |||||||
| chr4:44649392 | G | C | 1 | a0002c0003t0003g0101 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.116+593C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649392 | |||||||
| chr4:44649529 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG00741.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.116+456C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649529 | |||||||
| chr4:44649615 | T | TA | 46 | a0001c0001t0001g0094 a0001c0001t0001g0136 a0001c0002t0002g0011 others(43): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.116+369dupT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649615 | |||||||
| chr4:44649615 | TA | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(44): Show |
87 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.116+369delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649615 | |||||||
| chr4:44649624 | A | G | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.116+361T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649624 | |||||||
| chr4:44649647 | C | T | 1 | a0002c0003t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.116+338G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649647 | |||||||
| chr4:44649652 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0064 |
3 | HG02622.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.116+333C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649652 | |||||||
| chr4:44649693 | G | C | 1 | a0001c0001t0001g0035 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.116+292C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649693 | |||||||
| chr4:44649779 | A | G | 1 | a0001c0002t0002g0155 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.116+206T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649779 | |||||||
| chr4:44649803 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.116+182C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649803 | |||||||
| chr4:44649837 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.116+148C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649837 | |||||||
| chr4:44649940 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.116+45A>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649940 | |||||||
| chr4:44649949 | G | A | 1 | a0001c0002t0002g0225 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.116+36C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649949 | |||||||
| chr4:44649951 | C | CA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0039 others(21): Show |
40 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.116+33dupT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649951 | |||||||
| chr4:44649951 | CA | C | 7 | a0001c0002t0002g0028 a0001c0002t0002g0155 a0001c0002t0002g0156 others(4): Show |
9 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+33delT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 2/5 | chr4 | 44649951 | |||||||
| chr4:44650170 | C | G | 133 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(130): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.-1-69G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650170 | |||||||
| chr4:44650332 | G | C | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-231C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650332 | |||||||
| chr4:44650384 | C | T | 1 | a0002c0003t0001g0117 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-1-283G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650384 | |||||||
| chr4:44650443 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-342T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650443 | |||||||
| chr4:44650468 | C | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.-1-367G>A | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650468 | |||||||
| chr4:44650482 | G | GGCGCACA others(11): Show |
7 | a0001c0001t0001g0037 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
8 | HG02145.hp1 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-399_-1-382dupGC others(16): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650482 | |||||||
| chr4:44650487 | A | ACACACAT others(11): Show |
1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-1-404_-1-387dupCG others(16): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650487 | |||||||
| chr4:44650494 | T | TGC | 3 | a0001c0002t0002g0226 a0001c0002t0002g0227 a0001c0002t0002g0228 |
3 | HG02027.hp2 NA18980.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-1-395_-1-394dupGC | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650494 | |||||||
| chr4:44650494 | TGC | T | 20 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(17): Show |
36 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1-395_-1-394delGC | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650494 | |||||||
| chr4:44650498 | C | CGCT | 3 | a0001c0001t0001g0095 a0001c0002t0002g0096 a0001c0004t0002g0154 |
3 | NA18948.hp1 NA19054.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-1-398_-1-397insAG others(1): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650498 | |||||||
| chr4:44650500 | C | CA | 3 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0002c0003t0001g0152 |
3 | HG02559.hp1 HG02630.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-1-400_-1-399insT | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650500 | |||||||
| chr4:44650503 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-1-402C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650503 | |||||||
| chr4:44650504 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-1-403G>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650504 | |||||||
| chr4:44650505 | G | A | 20 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0064 others(17): Show |
40 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-1-404C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650505 | G | GCA | 14 | a0001c0001t0001g0094 a0001c0001t0001g0188 a0001c0002t0002g0044 others(11): Show |
16 | HG00733.hp2 HG01256.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-405_-1-404insTG | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650505 | G | GCACA | 3 | a0001c0001t0001g0213 a0001c0001t0004g0210 a0001c0002t0002g0175 |
3 | HG01978.hp2 HG03017.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-405_-1-404insTG others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650505 | G | GCACACA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0055 others(5): Show |
10 | HG00639.hp1 HG01123.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-405_-1-404insTG others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650505 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0214 |
3 | HG00642.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-405_-1-404insTG others(6): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650505 | GCGCA | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
70 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.-1-408_-1-405delTG others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650505 | |||||||
| chr4:44650507 | G | A | 67 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
96 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-1-406C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCA | 49 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0011 others(46): Show |
86 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-1-408_-1-407dupTG | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCACA | 30 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(27): Show |
33 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-410_-1-407dupTG others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCACACA | 5 | a0001c0001t0004g0053 a0001c0002t0002g0001 a0001c0002t0002g0016 others(2): Show |
6 | HG02717.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-412_-1-407dupTG others(4): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCACACAC others(3): Show |
2 | a0001c0001t0001g0123 a0001c0002t0002g0096 |
2 | NA19005.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-1-416_-1-407dupTG others(8): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0006 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-1-418_-1-407dupTG others(10): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCA | 6 | a0001c0002t0002g0001 a0001c0002t0002g0007 a0001c0002t0002g0011 others(3): Show |
8 | HG01346.hp2 HG01496.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCACAC others(3): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0121 a0001c0001t0001g0127 others(1): Show |
4 | NA18962.hp2 NA18971.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(8): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCACAC others(5): Show |
15 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
22 | HG00099.hp1 HG00609.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(10): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCACAC others(7): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0038 others(5): Show |
9 | HG00741.hp1 HG01070.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(12): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCACAC others(9): Show |
1 | a0001c0001t0001g0006 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-1-407_-1-406insTG others(14): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0006 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1-407_-1-406insTG others(8): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCGCAC others(7): Show |
2 | a0001c0001t0001g0134 a0001c0002t0002g0132 |
2 | HG01433.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(12): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCGCAC others(9): Show |
1 | a0001c0001t0001g0024 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-1-407_-1-406insTG others(14): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCGCAC others(11): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0038 |
2 | HG02615.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-1-407_-1-406insTG others(16): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | G | GCGCGCGC others(7): Show |
1 | a0001c0002t0002g0026 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-1-407_-1-406insTG others(12): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | GCA | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(1): Show |
8 | HG01993.hp2 HG02647.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-408_-1-407delTG | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650507 | GCACA | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(3): Show |
8 | HG00438.hp2 HG00673.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-410_-1-407delTG others(2): Show |
YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650507 | |||||||
| chr4:44650511 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-1-410T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650511 | |||||||
| chr4:44650642 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
8 | HG00639.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-541T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650642 | |||||||
| chr4:44650662 | G | A | 1 | a0001c0002t0002g0228 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-1-561C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650662 | |||||||
| chr4:44650991 | T | C | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+563A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44650991 | |||||||
| chr4:44651009 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+545C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651009 | |||||||
| chr4:44651024 | T | A | 95 | a0001c0001t0001g0030 a0001c0001t0001g0188 a0001c0001t0001g0213 others(92): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2+530A>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651024 | |||||||
| chr4:44651092 | A | G | 1 | a0001c0002t0002g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2+462T>C | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651092 | |||||||
| chr4:44651222 | T | C | 95 | a0001c0001t0001g0030 a0001c0001t0001g0188 a0001c0001t0001g0213 others(92): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2+332A>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651222 | |||||||
| chr4:44651397 | G | C | 181 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(178): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-2+157C>G | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651397 | |||||||
| chr4:44651501 | G | A | 9 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0230 others(6): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+53C>T | YIPF7 | ENSG00000177752.15 | transcript | ENST00000415895.9 | protein_coding | 1/5 | chr4 | 44651501 |